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ArticleRevista peruana de medicina experimental y salud publica2025

Genomic diversity of uropathogenic Escherichia coli in clinical isolates from six latin american countries, 2018-2023.

Francesca Caballero, Anne Martinez-Ventura, Diego Cuicapuza, Alex Fajardo-Loyola, Rosmery Gutierrez-Ajalcriña, Javier Soto-Pastrana, Percy Asmat-Marrufo, Evelyn Barco-Yaipen de Vera, Henry Meza-Fernandez, Mario Chambi-Quispe and 8 more

Abstract read
In one paragraph

Article in Revista peruana de medicina experimental y salud publica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Francesca CaballeroUniversidad Peruana Cayetano Heredia, Laboratorio de Genómica Microbiana, Lima, Perú.ORCID http://orcid.org/0009-0001-7241-4136
Anne Martinez-VenturaUniversidad Peruana Cayetano Heredia, Laboratorio de Genómica Microbiana, Lima, Perú.ORCID http://orcid.org/0009-0008-5271-4319
Diego CuicapuzaUniversidad Peruana Cayetano Heredia, Laboratorio de Genómica Microbiana, Lima, Perú.ORCID http://orcid.org/0000-0002-5735-4614
Alex Fajardo-LoyolaInstituto Nacional de Salud, Centro Nacional de Salud Pública, Laboratorio de Biotecnología y Biología molecular, Lima, Perú.ORCID http://orcid.org/0000-0002-8162-1321
Rosmery Gutierrez-AjalcriñaHospital de Huaycán, Área de Epidemiología, Lima, Perú.ORCID http://orcid.org/0000-0001-8237-6092
Javier Soto-PastranaHospital Nacional Docente Madre Niño San Bartolomé, Departamento de Patología Clínica, Área de Microbiología, Lima, Perú.ORCID http://orcid.org/0000-0001-9534-5746
Percy Asmat-MarrufoLaboratorio de Referencia Regional Salud Pública, Servicio de microbiología, Trujillo, La Libertad, Perú.ORCID http://orcid.org/0000-0003-3377-6713
Evelyn Barco-Yaipen de VeraHospital JAMO, Área de microbiología, Tumbes, Perú.ORCID http://orcid.org/0000-0002-9334-2661
Henry Meza-FernandezHospital Alberto Sabogal Sologuren, Departamento de Patología Clínica, Servicio de Microbiología, Bellavista, Callao, Perú.ORCID http://orcid.org/0000-0003-4973-7794
Mario Chambi-QuispeHospital Carlos Monge Medrano, Patología Clínica, Puno, Perú.ORCID http://orcid.org/0000-0003-3303-2087
Jimena Pino-DueñasHospital Regional del Cusco, Patología Clínica, Cusco, Perú.ORCID http://orcid.org/0000-0003-4563-5459
Nicomedes Laura-RivasLaboratorio de Referencia Regional de Salud Pública Huancavelica, Servicio de microbiología, Huancavelica, Perú.ORCID http://orcid.org/0000-0002-6413-3270
Alexander Briones-AlejoHospital Regional de Loreto, Servicio de microbiología, Iquitos, Perú.ORCID http://orcid.org/0000-0003-4849-6466
Pilar Diaz-RengifoLaboratorio de Referencia Regional Salud Pública San Martín, Servicio de Microbiología, Tarapoto, Perú.ORCID http://orcid.org/0000-0002-0929-4602
Carlos Peralta-SiesquenIPRESS Jorge Chávez, Área de microbiología, Madre de Dios, Perú.ORCID http://orcid.org/0000-0002-9605-8324
Guillermo SalvatierraUniversidad Peruana Cayetano Heredia, Laboratorio de Genómica Microbiana, Lima, Perú.ORCID http://orcid.org/0000-0002-6887-2599
Pablo TsukayamaUniversidad Peruana Cayetano Heredia, Laboratorio de Genómica Microbiana, Lima, Perú.ORCID http://orcid.org/0000-0002-1669-2553
Pool Marcos-CarbajalUniversidad Peruana Cayetano Heredia, Laboratorio de Genómica Microbiana, Lima, Perú.ORCID http://orcid.org/0000-0002-7741-0337

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMotivation for the study. To contribute to the genomic surveillance of UPEC in clinical samples from Latin America, in response to the growing public health problem represented by UTIs and their resistance to antimicrobials. Main findings. Our study revealed a high frequency of high-risk clones, such as ST131 and ST1193. Critical mutations were identified in genes associated with resistance to multiple antibiotics, including fluoroquinolones, beta-lactams, and fosfomycin. Implications. Our results highlight the urgent need to strengthen UPEC surveillance in Latin America. Tracking resistant strains and implementing measures to limit their spread is crucial and has a significant impact on the effectiveness of available treatments. OBJECTIVE.: To genetically characterize clinical isolates of uropathogenic Escherichia coli (UPEC) from hospitals in Peru and contextualize them against 127 additional UPEC genomes reported in six Latin American countries between 2018 and 2023. MATERIALS AND METHODS.: The genomes of 16 Peruvian UPEC isolates were sequenced, assembled and supplemented with 127 genomes available in the NCBI public database. Serotypes, sequence types (STs), antimicrobial resistance (AMR) genes, and resistance-associated mutations were identified. A phylogenetic analysis was also conducted in order to determine evolutionary relations and distribution in phylogroups. RESULTS.: The ST131 clone was the most prevalent (42.7%), followed by ST1193 (13.3%). Phylogroup B2 was widely predominant (83.2%), with serotype O25:H4 standing out. The resistance genes blaTEM-1, blaCTX-M-15, and blaCTX-M-27 were identified with high frequency, as well as mutations in gyrA and parC associated with fluoroquinolone resistance, especially in the ST131 clone. CONCLUSION.: Our findings show high circulation of high-risk UPEC clones, such as ST131 and ST1193, in Latin America, along with a notable burden of genes and mutations linked to multidrug resistance, highlighting the need to strengthen regional genomic surveillance.

backgroundMotivation for the study. To contribute to the genomic surveillance of UPEC in clinical samples from Latin America, in response to the growing public health problem represented by UTIs and their resistance to antimicrobials. Main findings. Our study revealed a high frequency of high-risk clones, such as ST131 and ST1193. Critical mutations were identified in genes associated with resistance to multiple antibiotics, including fluoroquinolones, beta-lactams, and fosfomycin. Implications. Our results highlight the urgent need to strengthen UPEC surveillance in Latin America. Tracking resistant strains and implementing measures to limit their spread is crucial and has a significant impact on the effectiveness of available treatments.

Indexed as

Escherichia coli InfectionsGenetic VariationUrinary Tract InfectionsUropathogenic Escherichia coliAnti-Bacterial AgentsDrug Resistance, Multiple, BacterialGenome, BacterialHumansLatin AmericaPeruPhylogenyAnti-Bacterial Agents

Identifiers

PMID40900482
PMCPMC12377891

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.